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载脂蛋白基因(rs266729)变异与成年肥胖患者代谢综合征和 2 型糖尿病的关系。

Relation of a variant in adiponectin gene (rs266729) with metabolic syndrome and diabetes mellitus type 2 in adult obese subjects.

机构信息

Department of Endocrinology and Nutrition, Endocrinology and Nutrition Research Center, School of Medicine, Hospital Clinico Universitario, University of Valladolid, Valladolid, Spain.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Oct;24(20):10646-10652. doi: 10.26355/eurrev_202010_23422.

Abstract

OBJECTIVE

Some studies in the literature indicate that ADIPOQ rs266729 polymorphism functionally regulates adiponectin promoter activity and secondarily adiponectin levels. The aim of the present investigation was to describe the association of rs266729 with diabetes mellitus (DM2), components of Metabolic syndrome (MS) and serum adiponectin levels.

PATIENTS AND METHODS

The study involved a population of 1004 adult obese subjects. Measurements of anthropometric parameters, blood pressure, fasting blood glucose, C-reactive protein (CRP), insulin concentration, insulin resistance (HOMA-IR), lipid profile, adipokines levels and prevalence of MS and DM2 were recorded. The genotype of ADIPOQ gene polymorphism (rs266729) was evaluated.

RESULTS

The distribution of the rs266729 polymorphism in this population was 56.7% (n=569) (CC), 33.1% (n=332) (CG) and 10.2% (n=103) (GG). Insulin and HOMA-IR levels were higher in G allele carriers than non G allele carriers. Adiponectin levels were lower in G allele carriers than non G allele carriers. In total group carriers of G allele, logistic regression analysis showed an increased risk of hyperglycaemia (OR=1.70, 95% CI=1.19-2.76, p=0.03) and prevalence of diabetes mellitus type 2 (OR=1.81, 95% CI=1.13-5.14, p=0.04), after adjusting by body mass index and age CONCLUSIONS: G allele of SNP (rs266729) of the ADIPOQ gene showed high values of insulin and HOMA-IR, and low values of adiponectin levels than non G allele carriers. G allele carriers showed higher rate of diabetes mellitus and hyperglycemia.

摘要

目的

一些文献研究表明,ADIPOQ rs266729 多态性在功能上调节脂联素启动子活性,并间接调节脂联素水平。本研究旨在描述 rs266729 与 2 型糖尿病(DM2)、代谢综合征(MS)成分和血清脂联素水平的相关性。

患者和方法

本研究纳入了 1004 名成年肥胖患者。记录了人体测量参数、血压、空腹血糖、C 反应蛋白(CRP)、胰岛素浓度、胰岛素抵抗(HOMA-IR)、血脂谱、脂联素水平以及 MS 和 DM2 的患病率。评估了 ADIPOQ 基因多态性(rs266729)的基因型。

结果

该人群中 rs266729 多态性的分布为 56.7%(n=569)(CC)、33.1%(n=332)(CG)和 10.2%(n=103)(GG)。G 等位基因携带者的胰岛素和 HOMA-IR 水平高于非 G 等位基因携带者。G 等位基因携带者的脂联素水平低于非 G 等位基因携带者。在总组携带者中,逻辑回归分析显示,血糖升高的风险增加(OR=1.70,95%CI=1.19-2.76,p=0.03),2 型糖尿病的患病率增加(OR=1.81,95%CI=1.13-5.14,p=0.04),在调整体重指数和年龄后。

结论

ADIPOQ 基因 SNP(rs266729)的 G 等位基因与非 G 等位基因携带者相比,具有较高的胰岛素和 HOMA-IR 值,较低的脂联素水平。G 等位基因携带者发生糖尿病和高血糖的几率更高。

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